Canonical Allele Identifier: CA1322085375

Gene: CD28

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203721043_203721044delinsAC , CM000664.2:g.203721043_203721044delinsAC	GRCh38
NC_000002.11:g.204585766_204585767delinsAC , CM000664.1:g.204585766_204585767delinsAC	GRCh37
NC_000002.10:g.204294011_204294012delinsAC	NCBI36
NG_029618.1:g.19569_19570delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324106.9:c.53-5590_53-5589delinsAC MANE Select	ENSP00000324890.7:n.53-5590_53-5589delinsAC
ENST00000324106.8:c.53-5590_53-5589delinsAC	ENSP00000324890.7:n.53-5590_53-5589delinsAC
ENST00000374481.7:c.53-8605_53-8604delinsAC	ENSP00000363605.4:n.53-8605_53-8604delinsAC
ENST00000458610.6:c.95-5590_95-5589delinsAC	ENSP00000393648.2:n.95-5590_95-5589delinsAC
NM_001243077.1:c.53-5590_53-5589delinsAC	NP_001230006.1:n.53-5590_53-5589delinsAC
NM_001243078.1:c.53-8605_53-8604delinsAC	NP_001230007.1:n.53-8605_53-8604delinsAC
NM_006139.3:c.53-5590_53-5589delinsAC	NP_006130.1:n.53-5590_53-5589delinsAC
XM_006712862.2:c.95-5908_95-5907delinsAC	XP_006712925.1:n.95-5908_95-5907delinsAC
XM_011512194.1:c.95-5590_95-5589delinsAC	XP_011510496.1:n.95-5590_95-5589delinsAC
XM_011512195.1:c.95-5590_95-5589delinsAC	XP_011510497.1:n.95-5590_95-5589delinsAC
XM_011512196.1:c.95-5590_95-5589delinsAC	XP_011510498.1:n.95-5590_95-5589delinsAC
XM_011512197.1:c.53-5590_53-5589delinsAC	XP_011510499.1:n.53-5590_53-5589delinsAC
XM_011512194.2:c.95-5590_95-5589delinsAC	XP_011510496.1:n.95-5590_95-5589delinsAC
XM_011512195.3:c.95-5590_95-5589delinsAC	XP_011510497.1:n.95-5590_95-5589delinsAC
XM_011512197.2:c.53-5590_53-5589delinsAC	XP_011510499.1:n.53-5590_53-5589delinsAC
NM_006139.4:c.53-5590_53-5589delinsAC MANE Select	NP_006130.1:n.53-5590_53-5589delinsAC
NM_001243077.2:c.53-5590_53-5589delinsAC	NP_001230006.1:n.53-5590_53-5589delinsAC
NM_001243078.2:c.53-8605_53-8604delinsAC	NP_001230007.1:n.53-8605_53-8604delinsAC